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United States · US · US:42961-122_dc86ba45-5462-4c1b-9a65-4bcf25e0e43b
First Aid Direct All Day Pain Relief
Orange BookUNIISPLATC G02CC02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerCintas Corporation
CountryUS (United States)
ATC codeG02CC02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc11429611220225 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01)
Annotations
UNII (FDA Substance ID)
9TN87S3A3C
NAPROXEN SODIUM
RxCUI 142442
Orange Book
A204872
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "9TN87S3A3C",
"rxcui": "142442",
"inchikey": "CDBRNDSHEYLDJV-FVGYRXGTSA-M",
"display_name": "NAPROXEN SODIUM",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"5258cef2-0e5c-4ccd-e063-6394a90a9e5c": {
"match": "brand_token",
"title": "FIRST AID ONLY LIDOCAINE HYDROCHLORIDE ANALGESIC BURN GEL (LIDOCAINE HYDROCHLORIDE) GEL [ACME UNITED CORPORATION]",
"spl_version": "1",
"published_date": "2026-06-02"
}
},
"productid": "42961-122_dc86ba45-5462-4c1b-9a65-4bcf25e0e43b",
"productndc": "42961-122",
"dosage_form": "TABLET, COATED",
"orange_book": {
"appl_no": "204872",
"products": [
{
"rs": false,
"rld": false,
"te_code": null,
"strength": "220MG",
"product_no": "001",
"approval_date": "Jan 23, 2017"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN OTC DRUG",
"substance_name": "NAPROXEN SODIUM",
"proprietary_name": "First Aid Direct All Day Pain Relief",
"active_ingred_unit": "mg/1",
"application_number": "ANDA204872",
"marketing_category": "ANDA",
"nonproprietary_name": "Naproxen Sodium",
"start_marketing_date": "20230719",
"active_numerator_strength": "220"
}Related drugs
Other records sharing ATC code G02CC02.
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